ENST00000413910.6:c.*135-11T>C
|
ENSP00000400542.2:n.*135-11T>C
|
|
ENST00000426673.6:c.*781-11T>C
|
ENSP00000407253.3:n.*781-11T>C
|
|
ENST00000484317.6:n.1613-11T>C
|
|
|
ENST00000492372.2:n.277-11T>C
|
|
|
ENST00000696575.1:c.1324-11T>C
|
ENSP00000512730.1:n.1324-11T>C
|
|
ENST00000696577.1:c.1339-11T>C
|
ENSP00000512731.1:n.1339-11T>C
|
|
ENST00000696578.1:c.*291-11T>C
|
ENSP00000512732.1:n.*291-11T>C
|
|
ENST00000696579.1:n.2343T>C
|
|
|
ENST00000696580.1:c.1252-11T>C
|
ENSP00000512733.1:n.1252-11T>C
|
|
ENST00000696581.1:c.*1313-11T>C
|
ENSP00000512734.1:n.*1313-11T>C
|
|
ENST00000696582.1:c.*545-11T>C
|
ENSP00000512735.1:n.*545-11T>C
|
|
ENST00000696583.1:c.1300-11T>C
|
ENSP00000512736.1:n.1300-11T>C
|
|
ENST00000696584.1:n.1863-11T>C
|
|
|
ENST00000696585.1:n.1982-11T>C
|
|
|
ENST00000696586.1:n.1756-11T>C
|
|
|
ENST00000696587.1:c.1219-11T>C
|
ENSP00000512737.1:n.1219-11T>C
|
|
ENST00000696588.1:c.730-11T>C
|
ENSP00000513251.1:n.730-11T>C
|
|
ENST00000696589.1:n.1114-11T>C
|
|
|
ENST00000696590.1:n.2354T>C
|
|
|
ENST00000696591.1:n.688-11T>C
|
|
|
ENST00000696592.1:n.3609T>C
|
|
|
ENST00000696627.1:c.*165-11T>C
|
ENSP00000512764.1:n.*165-11T>C
|
|
ENST00000696628.1:c.1339-11T>C
|
ENSP00000512765.1:n.1339-11T>C
|
|
ENST00000369550.10:c.1339-11T>C
MANE Select
|
ENSP00000358563.5:n.1339-11T>C
|
|
ENST00000369550.9:c.1339-11T>C
|
ENSP00000358563.5:n.1339-11T>C
|
|
ENST00000412124.5:c.597-11T>C
|
|
|
ENST00000426673.5:c.758-11T>C
|
|
|
ENST00000475966.1:n.828-11T>C
|
|
|
ENST00000492372.1:n.156-11T>C
|
|
|
ENST00000620277.4:c.*565-11T>C
|
ENSP00000478387.1:n.*565-11T>C
|
|
NM_001142463.2:c.1324-11T>C
|
NP_001135935.1:n.1324-11T>C
|
|
NM_001288747.1:c.*565-11T>C
|
NP_001275676.1:n.*565-11T>C
|
|
NM_001363.4:c.1339-11T>C
|
NP_001354.1:n.1339-11T>C
|
|
NR_110021.1:n.2040-11T>C
|
|
|
NR_110022.1:n.2159-11T>C
|
|
|
NR_110023.1:n.1933-11T>C
|
|
|
NM_001363.5:c.1339-11T>C
MANE Select
|
NP_001354.1:n.1339-11T>C
|
|
NM_001142463.3:c.1324-11T>C
|
NP_001135935.1:n.1324-11T>C
|
|
NR_110021.2:n.1918-11T>C
|
|
|
NR_110022.2:n.2037-11T>C
|
|
|
NR_110023.2:n.1811-11T>C
|
|
|
NM_001288747.2:c.*565-11T>C
|
NP_001275676.1:n.*565-11T>C
|
|